Macroevolution of plant defense strategies

Trends in Ecology and Evolution

Volumn 22, Issue 2, 2007, Pages 103-109

  Agrawal, Anurag A ^a  

^a Department of Obstetrics Gynecology   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COEVOLUTION; EVOLUTION; EVOLUTIONARILY STABLE STRATEGY; PHYLOGENETICS; PLANT DEFENSE; PLANT-HERBIVORE INTERACTION;

ANIMAL; ECOSYSTEM; EVOLUTION; GENETICS; INSECT; PHYLOGENY; PHYSIOLOGY; PLANT; PLANT PHYSIOLOGY; REVIEW;

ANIMALS; ECOSYSTEM; EVOLUTION; INSECTS; PHYLOGENY; PLANT PHYSIOLOGY; PLANTS;

INSECTA;

EID: 33846321889     PISSN: 01695347     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tree.2006.10.012     Document Type: Review

References (60)

1. Karban R., and Baldwin I.T. Induced Responses to Herbivory (1997), University of Chicago Press
2. Dethier V.G. Evolution of feeding preferences in phytophagous insects. Evolution 8 (1954) 32-54
3. Fraenkel G. The raison d'etre of secondary plant substances. Science 129 (1959) 1466-1470
4. Ehrlich P.R., and Raven P.H. Butterflies and plants: a study in coevolution. Evolution 18 (1964) 586-608
5. Janzen D.H. Tropical blackwater rivers, animals, and mast fruiting by the Dipterocarpaceae. Biotropica 6 (1974) 69-103
6. Feeny P.P. Plant apparency and chemical defense. In: Wallace J.W., and Mansell R.L. (Eds). Biochemical Interaction Between Plants and Insects (1976), Plenum Press 1-40
7. Coley P.D. Herbivory and defensive characteristics of tree species in a lowland tropical forest. Ecol. Monogr. 53 (1983) 209-233
8. van der Meijden E., et al. Defense and regrowth, alternative plant strategies in the struggle against herbivores. Oikos 51 (1988) 355-363
9. Agrawal A.A., et al. Ecological genetics of an induced plant defense against herbivores: additive genetic variance and costs of phenotypic plasticity. Evolution 56 (2002) 2206-2213
10. Hare J.D., et al. Costs of glandular trichomes in Datura wrightii: a three-year study. Evolution 57 (2003) 793-805
11. In: Fritz R.S., and Simms E.L. (Eds). Plant Resistance to Herbivores and Pathogens (1992), University of Chicago Press
12. Mauricio R., and Rausher M.D. Experimental manipulation of putative selective agents provides evidence for the role of natural enemies in the evolution of plant defense. Evolution 51 (1997) 1435-1444
13. Fornoni J., et al. Population variation in the cost and benefit of tolerance and resistance against herbivory in Datura stramonium. Evolution 58 (2004) 1696-1704
14. Armbruster W.S. Exaptations link evolution of plant-herbivore and plant-pollinator interactions: a phylogenetic inquiry. Ecology 78 (1997) 1661-1672
15. Nosil P., and Crespi B.J. Experimental evidence that predation promotes divergence in adaptive radiation. Proc. Natl. Acad. Sci. U. S. A. 103 (2006) 9090-9095
16. Murphy S.M. Enemy-free space maintains swallowtail butterfly host shift. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 18048-18052
17. Heil M., et al. Evolutionary change from induced to constitutive expression of an indirect plant resistance. Nature 430 (2004) 205-208
18. Singer M.S., and Stireman J.O. The tri-trophic niche concept and adaptive radiation of phytophagous insects. Ecol. Lett. 8 (2005) 1247-1255
19. Rehr S.S., et al. Chemical defence in Central American non-ant-acacias. J. Ecol. 42 (1973) 405-416
20. Heil M., et al. Reduced chemical defence in ant-plants? A critical re-evaluation of a widely accepted hypothesis. Oikos 99 (2002) 457-468
21. Steward J.L., and Keeler K.H. Are there trade-offs among antiherbivore defenses in Ipomoea (Convolvulaceae)?. Oikos 53 (1988) 79-86
22. Rudgers J.A., et al. Trade-offs among anti-herbivore resistance traits: insights from Gossypieae (Malvaceae). Am. J. Bot. 91 (2004) 871-880
23. Agrawal A.A., and Fishbein M. Plant defense syndromes. Ecology 87 (2006) S132-S149
24. Maddox G.D., and Root R.B. Structure of the encounter between goldenrod (Solidago altissima) and its diverse insect fauna. Ecology 71 (1990) 2115-2124
25. Berenbaum M.R., and Zangerl A.R. Phytochemical diversity: adaptation or random variation?. In: Romeo J.T., et al. (Ed). Phytochemical Diversity and Redundancy in Ecological Interactions (1996), Plenum Press 1-24
26. Kursar T.A., and Coley P.D. Convergence in defense syndromes of young leaves in tropical rainforests. Biochem. Syst. Ecol. 31 (2003) 929-949
27. Silvertown J., and Dodd M. Comparing plants and connecting traits. Phil. Trans. R. Soc. B 351 (1996) 1233-1239
28. Bustamante R.O., et al. Patterns of chemical defences in plants: an analysis of the vascular flora of Chile. Chemoecology 16 (2006) 145-151
29. Fine P.V.A., et al. Herbivores promote habitat specialization by trees in Amazonian forests. Science 305 (2004) 663-665
30. Fine P.V.A., et al. The growth-defense trade-off and habitat specialization by plants in Amazonian forests. Ecology 87 (2006) S150-S162
31. Coley P.D., et al. Divergent defensive strategies of young leaves in two species of Inga. Ecology 86 (2005) 2633-2643
32. Stamp N. Out of the quagmire of plant defense hypotheses. Q. Rev. Biol. 78 (2003) 23-55
33. Van Zandt, P.A. Plant defense, growth rate, and habitat: a comparative assessment of constitutive and induced resistance. Ecology (in press)
34. Becerra J.X. Insects on plants: macroevolutionary chemical trends in host use. Science 276 (1997) 253-256
35. Becerra J.X., et al. Interactions between chemical and mechanical defenses in the plant genus Bursera and their implications for herbivores. Am. Zool. 41 (2001) 865-876
36. Farrell B.D., and Mitter C. The timing of insect-plant diversification: might Tetraopes (Coleoptera: Cerambycidae) and Asclepias (Asclepiadaceae) have co-evolved?. Biol. J. Linnean Soc. 63 (1998) 553-577
37. Berenbaum M. Coumarins and caterpillars - a case for coevolution. Evolution 37 (1983) 163-179
38. Liscombe D.K., et al. Evidence for the monophyletic evolution of benzylisoquinoline alkaloid biosynthesis in angiosperms. Phytochemistry 66 (2005) 1374-1393
39. Wink M. Evolution of secondary metabolites from an ecological and molecular phylogenetic perspective. Phytochemistry 64 (2003) 3-19
40. Wink M., and Mohamed G.I.A. Evolution of chemical defense traits in the Leguminosae: mapping of distribution patterns of secondary metabolites on a molecular phylogeny inferred from nucleotide sequences of the rbcL gene. Biochem. Syst. Ecol. 31 (2003) 897-917
41. Farrell B.D., et al. Escalation of plant defense: do latex and resin canals spur plant diversification. Am. Nat. 138 (1991) 881-900
42. Nelson C.J., et al. Seasonal and intraplant variation of cardenolide content in the California milkweed Asclepias eriocarpa, and implications for plant defense. J. Chem. Ecol. 7 (1981) 981-1010
43. Agrawal A.A., and Kurashige N.S. A role for isothiocyanates in plant resistance against the specialist herbivore Pieris rapae. J. Chem. Ecol. 29 (2003) 1403-1415
44. Crisp M.D., and Cook L.G. Do early branching lineages signify ancestral traits?. Trends Ecol. Evol. 20 (2005) 122-128
45. Traw M.B., and Bergelson J. Interactive effects of jasmonic acid, salicylic acid, and gibberellin on induction of trichomes in Arabidopsis. Plant Physiol. 133 (2003) 1367-1375
46. Thaler J.S., and Karban R. A phylogenetic reconstruction of constitutive and induced resistance in Gossypium. Am. Nat. 149 (1997) 1139-1146
47. Agrawal A.A. Natural selection on common milkweed (Asclepias syriaca) by a community of specialized insect herbivores. Evol. Ecol. Res. 7 (2005) 651-667
48. Armbruster W.S., et al. Floral integration, modularity and accuracy: distinguishing complex adaptations from genetic constraints. In: Pigliucci M., and Preston K. (Eds). Phenotypic Integration: Studying the Ecology and Evolution of Complex Phenotypes (2004), Oxford University Press 23-49
49. Howe G.A. Jasmonates as signals in the wound response. J. Plant Growth Regul. 23 (2004) 223-237
50. Kliebenstein D.J., et al. Genetic architecture of plastic methyl jasmonate responses in Arabidopsis thaliana. Genetics 161 (2002) 1685-1696
51. Dudareva N., et al. Biochemistry of plant volatiles. Plant Physiol. 135 (2004) 1893-1902
52. Thaler J.S., et al. The role of the jasmonate response in plant susceptibility to diverse pathogens with a range of lifestyles. Plant Physiol. 135 (2004) 530-538
53. De Moraes C.M., et al. Herbivore-infested plants selectively attract parasitoids. Nature 393 (1998) 570-573
54. Herms D.A., and Mattson W.J. The dilemma of plants: to grow or defend. Q. Rev. Biol. 67 (1992) 283-335
55. Agrawal A.A. Plant defense and density dependence in the population growth of herbivores. Am. Nat. 164 (2004) 113-120
56. Janz N., and Nylin S. Butterflies and plants: a phylogenetic study. Evolution 52 (1998) 486-502
57. Becerra J.X. Synchronous coadaptation in an ancient case of herbivory. Proc. Natl. Acad. Sci. U. S. A. 100 (2003) 12804-12807
58. Funk D.J., et al. A history of host associations and evolutionary diversification for Ophraella (Coleoptera Chrysomelidae): new evidence from mitochondrial DNA. Evolution 49 (1995) 1008-1017
59. Ronquist F., and Liljeblad J. Evolution of the gall wasp-host plant association. Evolution 55 (2001) 2503-2522
60. Murphy S.M., and Feeny P.P. Chemical facilitation of a naturally occurring host shift by Papilio machaon butterflies (Papilionidae). Ecol. Monogr. 76 (2006) 399-414